Variant report

Variant	rs7436737
Chromosome Location	chr4:658089-658090
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:61 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	USF1	chr4:657851-658159	GM12878	blood:	n/a	n/a
2	POLR2A	chr4:657209-658164	GM15510	blood:	n/a	n/a
3	EGR1	chr4:657927-658119	GM12878	blood:	n/a	n/a
4	POLR2A	chr4:657857-658348	GM12891	blood:	n/a	n/a
5	EBF1	chr4:657790-658172	GM12878	blood:	n/a	chr4:657978-657989
6	TCF3	chr4:657862-658229	GM12878	blood:	n/a	n/a
7	MAX	chr4:657274-658234	H1-hESC	embryonic stem cell:	n/a	chr4:657449-657459
8	POLR2A	chr4:657356-658182	GM12878	blood:	n/a	n/a
9	MAX	chr4:657373-658204	GM12878	blood:	n/a	chr4:657449-657459
10	TBL1XR1	chr4:657909-658209	GM12878	blood:	n/a	n/a
11	TCF12	chr4:657926-658180	GM12878	blood:	n/a	chr4:658083-658093
12	POLR2A	chr4:657949-658115	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr4:657339-658233	GM12878	blood:	n/a	n/a
14	ZNF143	chr4:657896-658096	GM12878	blood:	n/a	chr4:658017-658027
15	ELF1	chr4:657736-658338	GM12878	blood:	n/a	n/a
16	POLR2A	chr4:657234-658353	H1-hESC	embryonic stem cell:	n/a	n/a
17	MXI1	chr4:656777-658347	SK-N-SH	brain:	n/a	n/a
18	MAX	chr4:657228-658269	H1-hESC	embryonic stem cell:	n/a	chr4:657449-657459
19	POLR2A	chr4:657261-658246	GM12891	blood:	n/a	n/a
20	POLR2A	chr4:657244-658126	GM18951	blood:	n/a	n/a
21	USF1	chr4:657457-658239	SK-N-SH_RA	brain:	n/a	chr4:657598-657609
22	GABPA	chr4:657227-658172	H1-hESC	embryonic stem cell:	n/a	chr4:658017-658026
23	E2F6	chr4:657344-658305	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr4:657079-658351	GM12878	blood:	n/a	n/a
25	POLR2A	chr4:657210-658217	GM18526	blood:	n/a	n/a
26	USF2	chr4:657469-658235	GM12878	blood:	n/a	n/a
27	ZBTB7A	chr4:657215-658107	ECC-1	luminal epithelium:	n/a	chr4:657487-657494
28	POLR2A	chr4:657839-658361	GM12878	blood:	n/a	n/a
29	GABPA	chr4:657764-658251	SK-N-SH	brain:	n/a	chr4:658017-658026
30	GABPA	chr4:657795-658204	H1-hESC	embryonic stem cell:	n/a	chr4:658017-658026
31	GABPA	chr4:657752-658418	MCF-7	breast:	n/a	chr4:658017-658026
32	USF1	chr4:657808-658144	SK-N-SH_RA	brain:	n/a	n/a
33	GABPA	chr4:657279-658371	SK-N-SH	brain:	n/a	chr4:658017-658026
34	POLR2A	chr4:657205-658301	Raji	blood:	n/a	n/a
35	BHLHE40	chr4:657291-658227	GM12878	blood:	n/a	n/a
36	USF1	chr4:657275-658143	H1-hESC	embryonic stem cell:	n/a	chr4:657598-657609
37	MAZ	chr4:657310-658193	GM12878	blood:	n/a	chr4:657449-657459
38	MTA3	chr4:657405-658185	GM12878	blood:	n/a	n/a
39	CHD2	chr4:657514-658193	H1-hESC	embryonic stem cell:	n/a	n/a
40	GABPA	chr4:657849-658243	GM12878	blood:	n/a	chr4:658017-658026
41	POLR2A	chr4:657362-658167	GM19193	blood:	n/a	n/a
42	E2F6	chr4:657230-658395	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr4:657298-658190	GM12878	blood:	n/a	n/a
44	POLR2A	chr4:657184-658258	GM12878	blood:	n/a	n/a
45	USF1	chr4:657786-658120	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr4:657181-658244	GM12878	blood:	n/a	n/a
47	PML	chr4:657750-658323	GM12878	blood:	n/a	n/a
48	GABPA	chr4:657888-658146	GM12878	blood:	n/a	chr4:658017-658026
49	MXI1	chr4:657947-658175	GM12878	blood:	n/a	n/a
50	USF2	chr4:657421-658144	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:658058-658108	AG10803	skin:	n/a
2	chr4:658058-658108	HMEC	breast:	n/a
3	chr4:658058-658108	GM12892	blood:	n/a
4	chr4:658058-658108	T-47D	breast:	n/a
5	chr4:658058-658108	ProgFib	skin:	n/a
6	chr4:658058-658108	ovcar-3	ovarian:	n/a
7	chr4:658058-658108	NB4	blood:	n/a
8	chr4:658058-658108	AG04449	skin:	fetal
9	chr4:658058-658108	HCF	heart:	n/a
10	chr4:658058-658108	SK-N-SH	brain:	n/a
11	chr4:658058-658108	SAEC	small airway:	n/a
12	chr4:658058-658108	RPTEC	kidney:	n/a
13	chr4:658058-658108	Jurkat	blood:	n/a
14	chr4:658058-658108	K562	blood:	n/a
15	chr4:658058-658108	HUVEC	blood vessel:	n/a
16	chr4:658058-658108	PANC-1	pancreas:	n/a
17	chr4:658058-658108	AoSMC	blood vessel:	n/a
18	chr4:658058-658108	HCPEpiC	choroid plexus:	n/a
19	chr4:658058-658108	HRCEpiC	kidney:	n/a
20	chr4:658058-658108	U87	brain:	n/a
21	chr4:658058-658108	SK-N-SH_RA	brain:	n/a
22	chr4:658058-658108	Hepatocyte	liver:	n/a
23	chr4:658058-658108	NT2-D1	testis:	n/a
24	chr4:658058-658108	MCF10A-Er-Src	breast:	n/a
25	chr4:658058-658108	HRPEpiC	eye:	n/a
26	chr4:658058-658108	AG09309	skin:	n/a
27	chr4:658058-658108	HNPCEpiC	eye:	n/a
28	chr4:658058-658108	GM19239	blood:	n/a
29	chr4:658058-658108	Caco-2	colon:	n/a
30	chr4:658058-658108	HCM	heart:	n/a
31	chr4:658058-658108	HRE	kidney:	n/a
32	chr4:658058-658108	PrEC	prostate:	n/a
33	chr4:658058-658108	HepG2	liver:	n/a
34	chr4:658058-658108	H1-hESC	embryonic stem cell:	embryo
35	chr4:658058-658108	MCF-7	breast:	n/a
36	chr4:658058-658108	NHBE	bronchial:	n/a
37	chr4:658058-658108	GM06990	blood:	n/a
38	chr4:658058-658108	HEEpiC	esophagus:	n/a
39	chr4:658058-658108	ECC-1	luminal epithelium:	n/a
40	chr4:658058-658108	NHDF-neo	bronchial:	n/a
41	chr4:658058-658108	A549	lung:	n/a
42	chr4:658058-658108	AG04450	lung:	fetal
43	chr4:658058-658108	BE2_C	brain:	n/a
44	chr4:658058-658108	HAEpiC	amniotic membrane:	n/a
45	chr4:658058-658108	GM12878	blood:	n/a
46	chr4:658058-658108	LNCaP	prostate:	n/a
47	chr4:658058-658108	HEK293	kidney:	embryo
48	chr4:658058-658108	SKMC	muscle:	n/a
49	chr4:658058-658108	HIPEpiC	eye:	n/a
50	chr4:658058-658108	GM12891	blood:	n/a

(count:1 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:644054..646414-chr4:656838..659721,2	MCF-7	breast:

No data

Variant related genes	Relation type
PDE6B	TF binding region
ENSG00000272927	TF binding region
ENSG00000272927	CpG island
PDE6B	CpG island
ENSG00000133256	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10027549	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10027866	0.93[MKK][hapmap]
rs10030136	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10031745	0.80[MKK][hapmap]
rs1135375	1.00[ASN][1000 genomes]
rs13119162	0.85[AFR][1000 genomes]
rs28374488	0.85[MKK][hapmap]
rs28407346	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28438498	0.89[MKK][hapmap]
rs28470912	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28483373	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28488910	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28525003	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28568555	1.00[ASN][1000 genomes]
rs28569875	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28573204	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28583078	1.00[CHD][hapmap];0.90[MKK][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28630797	1.00[ASN][1000 genomes]
rs28742266	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28742899	1.00[CHD][hapmap];0.81[LWK][hapmap];0.89[MKK][hapmap];0.87[YRI][hapmap];1.00[ASN][1000 genomes]
rs3864130	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs3864131	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3891250	1.00[CHD][hapmap];0.87[LWK][hapmap];0.90[MEX][hapmap];0.98[MKK][hapmap];0.85[YRI][hapmap];0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4463020	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4505760	0.85[MKK][hapmap]
rs4518182	1.00[ASN][1000 genomes]
rs58227539	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60316402	1.00[ASN][1000 genomes]
rs71602496	1.00[ASN][1000 genomes]
rs73056602	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73058406	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9985747	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9991613	0.84[CEU][hapmap];1.00[CHD][hapmap];0.90[MEX][hapmap];1.00[ASN][1000 genomes]
rs9992641	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv2830422	chr4:72247-681939	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv931097	chr4:72447-683874	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv878245	chr4:509178-694613	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
9	nsv878246	chr4:592507-696848	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
12	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
14	nsv593206	chr4:625962-735150	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
15	nsv878248	chr4:645300-685993	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
16	nsv878249	chr4:649639-691026	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
17	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs7436737	RP11-1191J2.2	cis	lung	GTEx
rs7436737	RP11-1191J2.2	cis	Thyroid	GTEx
rs7436737	ZNF721	cis	parietal	SCAN
rs7436737	RP11-1191J2.2	cis	Nerve Tibial	GTEx
rs7436737	POLN	cis	parietal	SCAN

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:656800-658200	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr4:656800-658200	Flanking Active TSS	Brain Hippocampus Middle	brain
3	chr4:656800-658200	Flanking Active TSS	Pancreas	Pancrea
4	chr4:656800-658400	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr4:656800-658400	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr4:656800-658400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:656800-658400	Active TSS	Fetal Intestine Large	intestine
8	chr4:656800-658800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:657000-658200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:657000-658200	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr4:657000-658200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr4:657000-658200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
13	chr4:657000-658200	Active TSS	Left Ventricle	heart
14	chr4:657000-658200	Bivalent/Poised TSS	Psoas Muscle	Psoas
15	chr4:657000-658200	Active TSS	Right Atrium	heart
16	chr4:657000-658200	Flanking Active TSS	Right Ventricle	heart
17	chr4:657000-658200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
18	chr4:657000-658200	Active TSS	NH-A	brain
19	chr4:657000-658400	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr4:657000-658400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:657000-658400	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr4:657000-658400	Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr4:657000-658400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr4:657000-658400	Active TSS	Primary T cells from cord blood	blood
25	chr4:657000-658400	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr4:657000-658400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr4:657000-658400	Flanking Active TSS	Fetal Brain Male	brain
28	chr4:657000-658400	Active TSS	Fetal Kidney	kidney
29	chr4:657000-658400	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr4:657000-658400	Active TSS	Fetal Lung	lung
31	chr4:657000-658600	Active TSS	H9 Cell Line	embryonic stem cell
32	chr4:657000-658600	Active TSS	GM12878-XiMat	blood
33	chr4:657200-658200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr4:657200-658200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:657200-658200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr4:657200-658200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:657200-658200	Active TSS	Colon Smooth Muscle	Colon
38	chr4:657200-658200	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr4:657200-658200	Flanking Active TSS	Esophagus	oesophagus
40	chr4:657200-658200	Active TSS	Ovary	ovary
41	chr4:657200-658400	Active TSS	H1 Cell Line	embryonic stem cell
42	chr4:657200-658400	Active TSS	Placenta Amnion	Placenta Amnion
43	chr4:657400-658200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr4:657400-658200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:657400-658200	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:657400-658200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr4:657400-658200	Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr4:657400-658200	Active TSS	Brain Angular Gyrus	brain
49	chr4:657400-658200	Active TSS	Sigmoid Colon	Sigmoid Colon
50	chr4:657400-658200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle

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